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Ammonia excretion in rainbow trout (Oncorhynchus mykiss): evidence for Rh glycoprotein and H⁺-ATPase involvement

¹ Department of Biology, McMaster University, Hamilton
² Department of Integrative Biology, University of Guelph, Guelph, Ontario, Canada
³ Ecofisiologia CIMAR, Porto, Portugal

	ABSTRACT

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Branchial ammonia transport in freshwater teleosts is not well understood. Most studies conclude that NH₃ diffuses out of the gill and becomes protonated to NH₄⁺ in an acidified gill boundary layer. Rhesus (Rh) proteins are new members of the ammonia transporter superfamily and rainbow trout possess genes encoding for Rh30-like1 and Rhcg2. We identified seven additional full-length trout Rh cDNA sequences: one Rhag and two each of Rhbg, Rhcg1, and Rh30-like. The mRNA expression of Rhbg, Rhcg1, and Rhcg2 was examined in trout tissues (blood, brain, eye, gill, heart, intestine, kidney, liver, muscle, skin, spleen) exposed to high external ammonia (HEA; 1.5 mmol/l NH₄HCO₃, pH 7.95, 15°C). Rhbg was expressed in all tissues, Rhcg1 was expressed in brain, gill, liver, and skin, and Rhcg2 was expressed in gill and skin. Brain Rhbg and Rhcg1 were downregulated, blood Rh30-like and Rhag were downregulated, and skin Rhbg and Rhcg2 were upregulated with HEA. After an initial uptake of ammonia into the fish during HEA, excretion was reestablished, coinciding with upregulations of gill Rh mRNA in the pavement cell fraction: Rhcg2 at 12 and 48 h, and Rhbg at 48 h. NHE2 expression remained unchanged, but upregulated H⁺-ATPase (V-type, B-subunit) and downregulated carbonic anhydrase (CA2) expression and activity were noted in the gill and again expression changes occurred in pavement cells, and not in mitochondria-rich cells. Together, these results indicate Rh glycoprotein involvement in ammonia transport and excretion in the rainbow trout while underscoring the significance of gill boundary layer acidification by H⁺-ATPase.

ammonia transport; gene expression; gill; Rhesus proteins

	INTRODUCTION

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THE CURRENT MODEL OF AMMONIA excretion from the freshwater teleost gill links NH₃ diffusion to CO₂ hydration (62). Expired CO₂ is converted to HCO₃^– and H⁺ by carbonic anhydrase (CA) in the gill mucus, and the resulting acidified gill boundary layer then traps NH₃ to NH₄⁺ (68, 69). In addition, this layer could also be acidified by H⁺ extruded from an apical vacuolar H⁺-ATPase (29, 30). However, as it is acidified, this boundary layer creates a microenvironment for a favorable transbranchial (blood-to-water) P_NH3 gradient that facilitates ammonia excretion. This is especially advantageous during exposure to high external ammonia (HEA), which reverses the normally positive ammonia gradient. Indeed, abolishing this layer with HEPES buffer during HEA reduces J_Amm (64).

Despite the dominance of this NH₃ diffusion-trapping theory, many past studies have supported the possibility of apical Na⁺/NH₄⁺ exchange (e.g., Refs. 26, 70). It has been argued, however, that freshwater cannot provide the Na⁺ gradients necessary to drive this exchange (62). Likewise, basolateral entry of NH₄⁺ into the gill via an Na⁺/NH₄⁺ exchanger (NHE) is unlikely since the electromotive force for Na⁺ is directed into the gill cytosol and NH₄⁺ cannot out-compete the much more abundant Na⁺ in the plasma for access to the NHEs (62). Also, no evidence exists to support basolateral ammonia transport via NH₄⁺ substitution for K⁺ on the Na⁺/K⁺-ATPase in the freshwater gill, although there are reports of this occurring in seawater fish (37, 50).

Ammonia transport has been studied for decades in microorganisms, but the molecular identity and function of potential transporters involved were not elucidated until recently. The genes and corresponding proteins were first identified as methylammonium permease (Mep) in yeast (41) and the ammonium transporter (Amt) in plants (48). Based on sequence similarity, mammalian homologs to the Mep/Amt proteins were identified as the Rh blood group-related proteins: Rh30 and the glycoproteins RhAG/Rhag, RhBG/Rhbg, and RhCG/Rhcg (19). The terminologies RhAG, RhBG and RhCG refer to human tissue, while Rhag, Rhbg, and Rhcg indicate nonhuman tissue (59). Rh30 and RhAG/Rhag are restricted to erythrocytes (RBCs), whereas RhBG/Rhbg and RhCG/Rhcg are expressed in various other tissues (19, 34, 35). The three glycoproteins conduct ammonia when expressed in heterologous systems, although disagreement exists as to whether NH₃ or NH₄⁺ is transported (22). The nonglycosylated Rh30 proteins form part of the Rh complex with RhAG on the RBC membrane, but their function is unknown (60, 61).

Rh proteins have been identified in different fish species (20, 21, 47), and functionally, it has been shown that pufferfish Takifugu rubripes Rh glycoproteins, like their mammalian counterparts, mediate the transport of the ammonium analog, methylammonium, when expressed in Xenopus oocytes (47). Recently we identified three Rh cDNA sequences in the unexposed and HEA-exposed mangrove killifish Kryptolebias marmoratus (21). HEA exposure resulted in upregulated Rh mRNA expression in the gill, liver, muscle, and skin. Two rainbow trout Rh genes (Rh30-like1 and Rhcg2) were identified in a previous study (20), but their tissue expression and potential involvement in ammonia transport have not been investigated.

With this background in mind, the objectives of this study were to identify and sequence Rh orthologs in the rainbow trout, to examine their expression pattern in different trout tissues under control conditions and when exposed to HEA, and to quantify the HEA-exposed gill expression of Rh orthologs as well as other proteins thought to be involved in the ammonia transport process.

	MATERIALS AND METHODS

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Animals
Rainbow trout [Oncorhynchus mykiss, Walbaum; 178–260 g], obtained from Humber Springs Trout Hatchery, Ontario, Canada were used for all experiments. The fish were held in dechlorinated Hamilton tap water (moderately hard: [Na⁺] = 0.6 mequiv/l, [Cl^–]=0.8 mequiv/l, [Ca²⁺] = 0.8 mequiv/l, [Mg²⁺] = 0.3 mequiv/l, [K⁺] = 0.05 mequiv/l; titration alkalinity 2.1 mequiv/l; pH 8.0; hardness 140 mg/l as CaCO₃ equivalents; temperature 12–16°C), and food was withheld for at least 1 wk prior to experimentation to stabilize the endogenous fraction of nitrogenous waste excretion (15). All fish were transferred to individual, darkened acrylic flux boxes supplied with aerated, continuously flowing dechlorinated tap water at 15 ± 0.5°C and allowed to recover overnight prior to experimentation. All procedures used were approved by the McMaster University Animal Research Ethics Board and are in accordance with the Guidelines of the Canadian Council on Animal Care.

HEA Experiment
Six fish were exposed to a nominal total ammonia (T_Amm) concentration of 1.5 mmol/l NH₄HCO₃ (pH 7.95 ± 0.05, 15.0 ± 0.5°C) for 12 or 48 h. Fluxes were conducted during which time the water flow was stopped and the box volume was set to 4 l. For the 48-h flux, a period of flow-through flushing was performed every 12 h to prevent toxic build-up of ammonia. Control fish (six each) were treated identically for 12 and 48 h without the addition of ammonia.

Water samples (10 ml) were taken at 12-h intervals, frozen at –20°C and later assayed in triplicate for T_Amm using a modified salicylate-hypochlorite method (58). After the flux periods, the fish were anesthetized with MS222 (0.1 g/l; Sigma, St. Louis, MO), and caudal blood was drawn into a heparinized syringe. Samples were centrifuged to separate plasma from RBCs (2 min, 20,000 g), immediately frozen in liquid nitrogen, stored at –70°C, and later analyzed enzymatically for plasma T_Amm (Raichem; Hemagen Diagnostics, San Diego, CA). Net flux rates of total ammonia (J_Amm, µmol·kg^–1·h^–1) were calculated as: J_Amm = (T_Ammi – T_Ammf) x V/(t x M), where i and f refer to initial and final concentration (µmol/l), V is water volume (L) in the box, t is the time elapsed (h), and M is the fish mass (kg). A negative J_Amm indicates a net excretion of ammonia to the water. A positive J_Amm indicates a net uptake of ammonia into the fish.

Sequencing and Characterization of Rainbow Trout Rh cDNAs
Tissue sampling.
Gill and blood samples for cloning purposes were removed from fish that were exposed to 1.5 mmol/l NH₄HCO₃ for 24 h. Control samples for all subsequent analyses were collected from fish that were held in individual flux boxes with flowing dechlorinated tap water for 24 h. Blood samples were collected (as described above) immediately after anesthetization and prior to tissue collection.

Preliminary studies indicated Rhbg expression on RBCs, so all analyses subsequent to cloning were performed on saline-perfused tissues to minimize the contribution of RBC mRNA to tissue levels. Samples of brain, eye, gill, heart, intestine, kidney, liver, muscle, skin, and spleen were removed after the fish were anaesthetized, placed on ice, and perfused free of blood with chilled, heparinized (50 IU/ml lithium heparin, Sigma) Cortland saline (66). Perfusions were performed by cannulation of the bulbus arteriosus with a 23-gauge butterfly needle attached to a peristaltic pump, and the ventricle was severed immediately after initiation of perfusion to allow for drainage. Tissue samples were immediately frozen in liquid nitrogen and stored at –70°C until analysis.

RNA extraction and reverse-transcriptase PCR amplification.
Total RNA was extracted from blood and tissues using TRIzol (Invitrogen, Burlington, ON, Canada), quantified spectrophotometrically, and electrophoresed on 1% agarose gels stained with ethidium bromide to verify integrity. First strand cDNA was synthesized from 1 µg total RNA using an oligo(dT₁₇) primer and Superscript II reverse transcriptase (Invitrogen). Samples were stored at –70°C.

Identification of Rh orthologs.
Partial Rh30-like, Rhag, Rhbg, and Rhcg1 sequences were obtained from cDNA of HEA-exposed blood or gill samples using primers (Table 1) designed from the trout Rh30-like1 sequence and pufferfish Rhag, Rhbg, and Rhcg2 sequences (GenBank: AY207445, AY618933, AY116074, AY116076, respectively). PCR were carried out in a PTC-200 MJ Research thermocycler with Taq DNA polymerase (Invitrogen) at 94°C (2 min) followed by 45 cycles of 94°C (30 s), 52°C (30 s), and 72°C (1 min). Products were electrophoresed on ethidium bromide-stained 1% agarose gels, and bands of appropriate size were excised and extracted using the Qiaquick gel extraction kit (Qiagen, Mississauga, ON, Canada). Purified gel products were ligated to a pGEM-T easy vector (Promega; Fisher Scientific, Nepean, ON, Canada), transformed into heat-shock competent Escherichia coli (XL-Blue; Stratagene, Mississauga, ON, Canada), and then grown on ampicillin LB agar plates. Colonies containing the ligated product were inoculated into liquid media and grown overnight. Plasmids were harvested using GeneJet Plasmid Miniprep Kit (Fermentas Canada, Burlington, ON, Canada), and sequencing was performed on an ABI 3100 Gene Analyzer at the MOBIX Lab, McMaster University (Hamilton, ON, Canada). Primers designed specific to the Rh orthologs (Table 1) were used to obtain full-length cDNA sequences by 5'- and 3'-5-rapid amplification of cDNA ends (Smart RACE cDNA amplification kit; BD Bioscience Clontech, Mississauga, ON, Canada). Several clones of the 3'- and 5'-ends were sequenced in both directions, and full-length transcripts were determined by majority-rule consensus with BioEdit (17). Sequences have been deposited into GenBank (Table 2).

Tissue distribution (PCR).
Following the methods described above, total RNA and cDNA were prepared from the RBCs and saline-perfused tissues collected from the initial HEA experiment. Distribution of Rh orthologs in control and HEA-exposed (48 h) tissues was determined using ortholog-specific primers (Table 1) with the PCR protocol described earlier. Products were electrophoresed on ethidium bromide-stained 1.5% agarose gels.

Tissue expression (quantitative real-time PCR).
Rh expression in tissues exposed to HEA for 12 and 48 h was compared with control tissues by quantitative real-time PCR (qPCR) using the cDNA prepared above and ortholog-specific primers (Table 1). Primer specificity was confirmed in preliminary experiments, and qPCR analyses were performed on an Mx3000P QPCR System (Stratagene, Cedar Creek, TX). Reactions (20 µl) containing 4 µl of DNaseI-treated (Invitrogen) cDNA, 4 pmol of each primer, 10 µl of Platinum SYBR Green qPCR SuperMix-UDG (Invitrogen), and 0.8 µl of ROX (1:10 dilution) were performed at 50°C (2 min), 95°C (2 min), followed by 40 cycles of 95°C (15 s) and 60°C (30 s). Melt-curve analysis confirmed production of a unique product, and gel electrophoresis verified presence of a single band. A nonreversed-transcribed sample controlled for possible genomic DNA contamination. Elongation factor-1 (EF-1, GenBank AF498320) for gill and ß-actin (GenBank AF157514) for other tissues had the most stable expression across samples and were used as endogenous standards to calculate relative mRNA expression by the standard curve method. Standard curves were generated by serial dilution of a random mixture of control samples. To discriminate between erythroid and nonerythroid Rhbg mRNA expression, unperfused samples of brain, kidney, and liver were analyzed and compared with samples that had been perfused free of blood, by the same methods as those described earlier.

Pavement cell and mitochondria-rich cell expression.
Pavement and mitochondria-rich (MR) cells were isolated from gill epithelial cells using a technique modified from Galvez et al. (16). Whole branchial baskets were removed from control and HEA-exposed fish, and gill filaments were trypsin-digested, passed through 96-µm filters, treated with RBC lysis buffer and layered onto a discontinuous Percoll density gradient. Pavement cells were harvested from the 1.03–1.05 g/ml interface, and MR cells were harvested from the 1.05–1.09 g/ml interface. Total RNA and cDNA were processed as described above from both cell fractions, and the mRNA expression of Rh was measured relative to ß-actin.

Enzyme/Transporter Expression in the Gill
Following the qPCR protocol outlined earlier, expression of H⁺-ATPase (V-type, B subunit; GenBank AF14002), carbonic anhydrase (cytoplasmic, CA2; GenBank AY514870), four isoforms of Na⁺/K⁺-ATPase (1a, 1b, 1c, 3; GenBank: AY319391, AY319390, AY319387, AY319388), and NHE2 (GenBank EF446605) was quantified in control and HEA-exposed whole gill samples relative to EF-1, and in control and HEA-exposed pavement and MR cells relative to ß-actin. Expression of Na⁺/K⁺-ATPase isoforms 1a and 1b were quantified in the gill cell fractions, but as the results were similar, only the results of 1a are reported here.

Enzyme Activity in the Gill
Enzyme assays were performed in triplicate on homogenates of gill tissues that were perfused free of blood, extracted, and frozen from the previous HEA experiment. Protein assays were performed using Bradford Reagent (Sigma) and BSA standards.

ATPase activity.
Protocols for Na⁺/K⁺-ATPase (44) and H⁺-ATPase (32) assays were modified and adapted to measure activity levels in control and HEA-exposed fish gills. Activities are reported as control activity (no inhibitor) minus inhibitor-treated activity [ouabain for Na⁺/K⁺-ATPase and sodium azide with N-ethylmaleimide (NEM) for V-type H⁺-ATPase], measured at 340 nm in a kinetic microplate reader (SpectraMAX Plus; Molecular Devices, Menlo Park, CA) at 15-s intervals for 30 min. We obtained the same results for H⁺-ATPase activity using 10 µM bafilomycin as an inhibitor but are only reporting results obtained using NEM.

CA.
CA activity was determined using the electrometric pH method (18). Briefly, samples were assayed in a pH 7.4 buffer (225 mmol mannitol, 75 mmol sucrose, 10 mmol Tris) held at 4°C, and the reaction was initiated with 200 µl of CO₂-saturated water. The reaction velocity was measured, using hydrogen and reference electrodes (Kwik-Tip; World Precision Instruments, Sarasota, FL) attached to an Accumet XL15 pH meter (Fisher Scientific), over a 0.15 pH change, and the activity is reported as the observed rate minus the uncatalyzed rate.

Statistical Analysis
All data are presented as means ± SE (n, number of fish). Values at each time point were compared with control values using one-way analysis of variance with Fisher's least significant difference post hoc test. Student's t-test was used for comparisons of T_Amm and J_Amm values and for comparisons between unperfused and perfused tissues. Significance was set at = 0.05.

	RESULTS

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HEA Experiment
Exposure to HEA initially resulted in net uptake of ammonia from the water into the fish during the first 12 h. Thereafter, net excretion of ammonia occurred and by 48 h, J_Amm exceeded the 12- and 48-h control rates, which remained unchanged (Fig. 1). Plasma T_Amm levels in HEA-exposed fish were significantly higher than the control value (Fig. 2), but they remained lower than water levels throughout the time course. There is however, a noticeable upward trend toward 48 h approaching a toxic level (36), but no signs of stress were visible in these fish.

View larger version (10K): [in this window] [in a new window]   Fig. 1. The effect of 48 h of exposure to 1.5 mmol/l NH4HCO3 on net ammonia flux (JAmm). Negative values indicate excretion; positive values represent uptake. *Significantly different from the 12- and 48-h controls (0 mmol/l NH4HCO3). Control values are not significantly different from each other (P < 0.05). Data are means ± SE (n = 6–12).

View larger version (10K): [in this window] [in a new window]   Fig. 2. The effect of 48 h of exposure to 1.5 mmol/l NH4HCO3 on water and plasma total ammonia (TAmm). *Plasma values significantly different from water values (P < 0.05). Data are means ± SE (n = 6–12).

View larger version (28K): [in this window] [in a new window]   Fig. 3. An unrooted phylogenetic tree of Rh homolog sequences in fish. Numbers represent bootstrap values from 500 replicates. Accession numbers appear in parentheses. *Sequences identified in this study.

View larger version (79K): [in this window] [in a new window]   Fig. 4. Amino acid sequence alignments of fish Rh homologs. Accession numbers appear in parentheses. *Sequences identified in this study.

View larger version (23K): [in this window] [in a new window]   Fig. 5. Hydropathy profile of rainbow trout Rhbg. Gray boxes indicate predicted transmembrane regions.

View larger version (14K): [in this window] [in a new window]   Fig. 6. Tissue distribution of Rh glycoproteins as determined by PCR in rainbow trout exposed to 0 mmol/l NH4HCO3 (A) and 1.5 mmol/l NH4HCO3 (B). These gels show qualitative rather than quantitative expression; n = 3 for each Rh ortholog and treatment.

View larger version (12K): [in this window] [in a new window]   Fig. 7. mRNA expression of Rhbg relative to ß-actin in the blood and the unperfused and perfused brain, kidney, and liver of rainbow trout exposed to 0 mmol/l NH4HCO3 (control) and 1.5 mmol/l NH4HCO3 for 48 h. *Significant difference between control and 48-h perfused brain (P < 0.05). Data are means ± SE (n = 6).

View larger version (9K): [in this window] [in a new window]   Fig. 8. mRNA expression of Rhbg, Rhcg1, and Rhcg2 relative to elongation factor (EF)-1 expression in the gills of rainbow trout exposed to 1.5 mmol/l NH4HCO3 for 12 and 48 h *Significant differences from the control (P < 0.05). Data are means ± SE (n = 6).

View larger version (8K): [in this window] [in a new window]   Fig. 9. mRNA expression of Rhbg, Rhcg1, and Rhcg2 relative to ß-actin in the skin of rainbow trout exposed to 1.5 mmol/l NH4HCO3 for 12 and 48 h. *Significant differences from the control (P < 0.05). Data are means ± SE (n = 6).

View larger version (8K): [in this window] [in a new window]   Fig. 10. mRNA expression of Rhcg1 relative to ß-actin in the brain and liver of rainbow trout exposed to 1.5 mmol/l NH4HCO3 for 12 and 48 h. *Significant differences from the control (P < 0.05). Data are means ± SE (n = 6).

Gill cell fractionation was performed to ascertain the cellular location of these changes in expression. In the pavement cell fraction, there was no change in Rhcg1 expression, but there was a 4.3-fold increase in Rhbg expression at 48 h of HEA and an 8.1 and 10.8-fold increase in Rhcg2 expression at 12 and 48 h of HEA, respectively (Fig. 11A). No significant changes in Rh mRNA expression were noted in the MR cell fraction, though Rhcg1 expression tended to fall (Fig. 11B).

View larger version (12K): [in this window] [in a new window]   Fig. 11. mRNA expression of Rhbg, Rhcg1, and Rhcg2 relative to ß-actin in pavement cells (A) and mitochondria-rich cells (B) isolated from the gills of rainbow trout exposed to 1.5 mmol/l NH4HCO3 for 12 and 48 h. *Significant differences from the control (P < 0.05). Data are means ± SE (n = 6).

View larger version (10K): [in this window] [in a new window]   Fig. 12. mRNA expression of Rh30-like2 , Rh30-like3, and Rhag relative to ß-actin in the red blood cells (RBCs) from rainbow trout exposed to 1.5 mmol/l NH4HCO3 for 12 and 48 h. *Significant differences from the control (P < 0.05). Data are means ± SE (n = 6).

View larger version (14K): [in this window] [in a new window]   Fig. 13. mRNA expression relative to EF-1 of H+-ATPase (A), carbonic anhydrase (CA2, B), and Na+/K+-ATPase -subunit isoforms (C) and the enzyme activities of H+-ATPase (D), carbonic anhydrase (E), and Na+/K+-ATPase (F) in the gills of rainbow trout exposed to 1.5 mmol/l NH4HCO3 for 12 and 48 h. *Significant differences from the control (P < 0.05). Data are means ± SE (n = 6).

View larger version (13K): [in this window] [in a new window]   Fig. 14. mRNA expression relative to ß-actin of carbonic anhydrase, H+-ATPase, NHE2, and Na+/K+-ATPase (1a) in pavement cells (A) and mitochondria-rich cells (B). *Significant differences from the control (P < 0.05). Data are means ± SE (n = 6).

	DISCUSSION

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All sequences identified in this study have 12 predicted transmembrane domains, a highly conserved characteristic observed in the Rh protein family (19). The Rh30-like1 and Rh30-like2 sequences are identical, with the exception of a single amino acid deletion and four amino acid substitutions in Rh30-like1 (Fig. 4). Rh30-like2 and Rh30-like3 differ only at the 3'-end due to a 73-base pair (bp) deletion in Rh30-like2. We also identified a partial Rh30-like4 sequence with a more varied CDS as well as two variants of Rhag lacking the 12 predicted transmembrane spanning domains typical of the other Rh family members.

These multiple Rh30-like and Rhag sequences are likely the result of polyploidization events that occurred in the lineage leading to modern ray-finned fishes (65). Salmonids have further undergone a recent (25–100 million years ago) tetraploidization event (1), resulting in duplicated genes. Indeed, multiple Wilms' tumor suppressor (5) and glutamine synthetase (46) genes in trout are likely the result of both ancient and recent duplication events. It is possible, therefore, that additional (yet unidentified) Rh genes will be characterized in the future.

The cDNA sequences of Rhbg-a and Rhbg-b are identical with the exception of a 474-bp deletion in the 3'-UTR of Rhbg-b. Rhcg1-a and Rhcg1-b are also identical, except for a 299-bp deletion in the 3'-UTR of Rhcg1-b. Presumably the two Rhbg sequences are RNA splice variants from the same gene, and this is likely the case for the two Rhcg1 sequences. Although we cannot speculate about the function of the Rhbg and Rhcg1 variants, it is reasonable to conclude that they are differentially expressed given that 3'-UTRs are important for posttranscriptional regulation (43). Furthermore, preliminary results using primers designed specifically to Rhbg-a suggest that the Rhbg expression changes that we report here in the brain and skin (Figs. 7 and 9) likely reflect changes in Rhbg-b.

Both Rhbg and Rhcg1 are very similar (>75%) to their counterparts in other fish species, but there is more variability between the Rh30-like sequences (Fig. 4). The Rh30-like sequences fall into a cluster of homologs related to the Rh30 proteins (Fig. 3) that were first described in humans (3). There is 60% amino acid similarity between trout Rhbg/Rhcg and human RhBG/RhCG, but trout Rh30-like sequences are <31% similar to human Rh30 (not shown). This agrees well with Huang and Peng (20), who showed that Rh30 is more functionally divergent across species than the other Rh genes. Rh30 proteins do not directly transport ammonia, but their membrane expression depends on the presence of RhAG (60). In the present study, the mRNA expression of Rh30-like and Rhag followed the same pattern of downregulation in HEA-exposed RBCs (Fig. 12), suggesting that these proteins could also be coexpressed together on the trout RBC membrane. Whether Rhag is additionally expressed in pillar cells of the trout gill, as they are in the pufferfish (47), remains to be determined.

Exposure to 1.5 mmol/l NH₄HCO₃ for 48 h resulted in an initial net uptake of ammonia into the fish with subsequent recovery of excretion (Fig. 1). This is consistent with earlier investigations that reported the same phenomenon in both freshwater and seawater fish exposed to high (up to 1 mmol/l) external concentrations of NH₄Cl or (NH₄)₂SO₄ (6, 7, 8, 63). These studies hypothesized that an active NH₄⁺ extrusion mechanism is induced to counteract the inward diffusion of NH₃, but active NH₄⁺ exchange has not yet been demonstrated in the freshwater teleost gill, leaving NH₃ diffusion as the main route of excretion (54, 62).

The lipid solubility of NH₃ is, however, only moderate at best (13, 67), and a protein channel would greatly facilitate NH₃ passage even under routine conditions. This is particularly advantageous when potentially toxic concentrations of ammonia need to be transported out quickly. In HEA conditions, fish need to counter the influx of ammonia as well as eliminate endogenously produced ammonia. This became apparent at 48 h of HEA when plasma T_Amm approached water T_Amm (Fig. 2). Recovery of excretion after 12 h, and the increased J_Amm at 48 h (Fig. 1) was accompanied by the simultaneous upregulation of Rhcg2 at 12 and 48 h (Fig. 8). This suggests that Rhcg2 is upregulated in response to HEA, resulting in enhanced ammonia excretion.

Although Rhcg2 was upregulated during HEA, all three Rh mRNAs (Rhbg, Rhcg1, and Rhcg2) were expressed in the whole gill and gill cell fractions during control and HEA conditions (Figs. 8 and 11). Analysis of the gill cell fractions revealed that Rhcg2 upregulation at 12 and 48 h was accompanied by Rhbg upregulation at 48 h and that these changes were occurring in the pavement cells and not in MR cells (Fig. 11). Taken together, this suggests that while both cell types may be involved in routine ammonia transport via Rh glycoproteins during control and HEA conditions, pavement cells respond to HEA with an upregulation of Rhcg2, restoring excretion and elevating rates above basal levels. Rhbg may be involved in the maintenance or further regulation of this process. These ideas still need to be validated with trout-specific Rh protein studies, which will reveal whether changes in Rh protein levels or subcellular distribution occur as they do in rat renal cells during metabolic acidosis (55).

In the gill of the pufferfish, localization of Rh mRNAs and proteins suggests that at least under basal conditions, Rhcg1 is expressed apically and is confined to the MR cells while Rhcg2 and Rhbg are restricted to pavement cells in the apical and basolateral regions, respectively (47). In the gills of the rainbow trout, on the other hand, our findings show that the trout Rh mRNAs are expressed in both the MR and pavement cells under control conditions but respond differentially under HEA: Rhbg and Rhcg2 expression increases in pavement cells only, while Rhcg1 expression does not change in pavement cells but tends to fall in MR cells. Whether this discrepancy in findings is due to species differences and whether or not the same polarized localization of Rh glycoproteins occurs in the trout gill await further investigation.

Previous studies demonstrated that expired water passing over the gills of freshwater fish is acidified by up to 1.5 pH units, depending on initial water pH and buffer capacity (30, 49, 69). This acidified gill boundary layer traps excreted NH₃ to NH₄⁺ (51, 64), but whether the acidification is due to H⁺ arising from CO₂ hydration or is a result of H⁺ extruded by H⁺-ATPase is unknown (62). In our study, an increase in H⁺-ATPase expression and activity (Fig. 13, A and D) accompanied the Rhcg2 upregulation and recovery of ammonia excretion during HEA, suggesting that H⁺-ATPase is responsible for the acidification. Moreover, this upregulation of H⁺-ATPase occurred in the pavement cells (Fig. 14), indicating a possible functional coupling with Rhcg2, which has also been hypothesized to occur in the intercalated cells of the rat nephron (11).

The CA-catalyzed hydration of CO₂ normally fuels the H⁺-ATPase with H⁺ in the trout gill (31), so we expected to see an increase in CA expression and/or activity in conjunction with the upregulated H⁺-ATPase in HEA conditions. Instead, CA expression and activity were significantly decreased at 48 h (Fig. 13, B and E), a response that again appeared specific to the pavement cells (Fig. 14), in agreement with one study that reported inhibition of CA activity by HEA in trout (2). Downregulation or lowered CA activity suggests that CO₂ is no longer the main source of H⁺ for the H⁺-ATPase pump. Under ammonia-loaded conditions, NH₄⁺ may be the major supplier of H⁺. This correlates with the present model of the ammonium transporter (AmtB) of E. coli, which is structurally and functionally similar to Rh proteins (9, 38, 72). AmtB is a trimeric membrane-spanning complex (10, 24, 71) functioning as an NH₃ channel. The NH₄⁺ is deprotonated before entering the channel so that it can pass through as NH₃ and reprotonate after exiting (24, 25). Under HEA, a continuous and abundant supply of H⁺ stripped off from NH₄⁺ entering the Rh channel may be fuelling the H⁺-ATPase (Fig. 15), making elevated CA activity unnecessary.

View larger version (8K): [in this window] [in a new window]   Fig. 15. Schematic diagram of a gill cell showing Rhcg2-mediated NH3 transport coupled to active H+ secretion. The result is a net excretion of NH4+ across the apical gill epithelium.

Results from this study revealed a wide tissue expression of Rh mRNAs with a noted downregulation of Rhbg and Rhcg1 occurring in the brain with HEA exposure (Figs. 7 and 10). Since trout brain cells have only a limited capacity to detoxify ammonia (45), we could hypothesize that this downregulation of Rh was a protective response to prevent ammonia overloading into the cells. Downregulation of Rhbg did not occur in the mangrove killifish brain in response to similar HEA conditions (21), and this may reflect species differences: the mangrove killifish is very ammonia tolerant (14) compared with the trout (45). Interestingly, Rh glycoproteins were not detected in the pufferfish brain (47).

During HEA, Rhbg and Rhcg2 were upregulated in the skin (Fig. 9). This was surprising as the skin under normal conditions contributes very little to total ammonia excretion in freshwater teleosts compared with seawater species (67). Upregulation of Rhcg1 and Rhcg2 was also observed in the mangrove killifish skin exposed to HEA or air (21). This species, however, is known to volatilize ammonia via the skin during air exposure (33). Whether the trout skin also assumes an excretory role during HEA is not clear, but Rh proteins appear to play some role in this tissue during HEA.

An important controversy regarding the function of Rh proteins is whether or not they transport CO₂. Chlamydomonas reinhardtii is a green algae with Amt and Rh (Rh1) genes. When Rh1 is inhibited, ammonium uptake is unaffected but the growth increase that normally occurs in high CO₂ is impaired. Elevating the CO₂ content of the growth medium increases Rh1 expression (28, 56). Also, RBCs lacking RhAG (Rh_null) have reduced CO₂ permeability (12), and RhCG-expressing oocytes have increased CO₂ permeability (4). Contrary to this, however, Ripoche et al. (53) reported no change in CO₂ permeability in Rh_null ghost cell preparations. Future studies should include investigations into the potential CO₂ transport via Rh proteins.

In summary, we identified seven full-length Rh cDNA sequences in the rainbow trout and evaluated the gene expression of these as well as Rhcg2 at the transcript level in the rainbow trout challenged with HEA. Rh mRNAs were expressed in many tissues, and changes in expression upon HEA exposure were noted in some. In the gill, the main site of ammonia excretion, Rhcg2 expression as well as H⁺-ATPase expression and activity were upregulated during HEA and this coincided with the net recovery of ammonia excretion. CA expression and activity were significantly downregulated at 48 h of HEA, suggesting that CA is no longer fuelling the H⁺-ATPase pump at this point. Furthermore, pavement cells and not MR cells appear to be instrumental in the regulation of ammonia transport during HEA since clear expression changes in Rh and enzymes were occurring in this cell type only. The contribution of Rh glycoproteins and H⁺-ATPase to enhanced ammonia excretion across the gill during HEA has been highlighted, adding to our current knowledge and understanding of branchial ammonia transport in the freshwater rainbow trout.

	GRANTS

TOP ABSTRACT INTRODUCTION MATERIALS AND METHODS RESULTS DISCUSSION GRANTS REFERENCES

 
Funded by the Natural Sciences and Engineering Research Council of Canada Discovery Grants and Canada Foundation for Innovation/Ontario Innovation Trust equipment awards to C. M. Wood and P. A. Wright. C. M. Wood is supported by the Canada Research Chair Program.

	ACKNOWLEDGMENTS

 
We thank Richard Smith, Paul Craig, and Grant McClelland for logistic support and three anonymous reviewers for constructive criticisms.

	FOOTNOTES

 
Address for reprint requests and other correspondence: C. M. Nawata, Dept. of Biology, McMaster Univ., 1280 Main St. W., Hamilton, Ontario, Canada, L8S 4K1 (e-mail: nawatacm{at}mcmaster.ca).

	REFERENCES

TOP ABSTRACT INTRODUCTION MATERIALS AND METHODS RESULTS DISCUSSION GRANTS REFERENCES

 

1. Allendorf FW, Thorgaard GH. Tetraploidy and the evolution of salmonid fishes. In Evolutionary Genetics of Fishes edited by Turner BJ. New York: Plenum Press, 1984, p. 1–46.
2. ArasHisar S, Hisar O, Yanik T, Aras SM. Inhibitory effects of ammonia and urea on gill carbonic anhydrase enzyme activity of rainbow trout (Oncorhynchus mykiss). Env Tox Pharm 17: 125–128, 2004.[CrossRef]
3. Avent ND, Reid ME. The Rh blood group system: a review. Blood 95: 375–387, 2000.[Abstract/Free Full Text]
4. Bakouh N, Benjelloun F, Hulin P, Brouillard F, Edelman A, Chérif-Zahar B, Planelles G. The challenge of understanding ammonium homeostasis and the role of Rh glycoproteins. Tranfus Clin Biol 13: 139–146, 2006.[CrossRef]
5. Brunelli JP, Robison BD, Thorgaard GH. Ancient and recent duplications of the rainbow trout Wilms' tumor gene. Genome 44: 455–462, 2001.[Medline]
6. Cameron JN. Responses to reversed NH₃ and NH₄⁺ gradients in a teleost (Ictalurus punctatus), an elasmobranch (Raja erinacea), and a crustacean (Callinectes sapidus): evidence for NH₄⁺/H⁺ exchange in the teleost and the elasmobranch. J Exp Zool 239: 183–195, 1986.[CrossRef][Web of Science][Medline]
7. Cameron JN, Heisler N. Studies of ammonia in the trout: physico-chemical parameters, acid-base behaviour and respiratory clearance. J Exp Biol 105: 107–125, 1983.[Abstract/Free Full Text]
8. Claiborne JB, Evans DH. Ammonia and acid-base balance during high ammonia exposure in a marine teleost (Myoxocephalus octodecimspinosus). J Exp Biol 140: 889–105, 1988.
9. Conroy MJ, Bullough PA, Merrick M, Avent ND. Modelling the human rhesus proteins: implications for structure and function. Br J Haematol 131: 543–551, 2005.[CrossRef][Web of Science][Medline]
10. Conroy MJ, Jamieson SJ, Blakey D, Kaufmann T, Engel A, Fotiadis D, Merrick M, Bullough PA. Electron and atomic force microscopy of the trimeric ammonium transporter AmtB. EMBO Rep 5: 1153–1158, 2004.[CrossRef][Web of Science][Medline]
11. Eladari D, Cheval L, Quentin F, Bertrand O, Mouro I, Cherif-Zahar B, Cartron JP, Paillard M, Doucet A, Chambrey R. Expression of RhCG, a new putative NH₃/NH₄⁺ transporter, along the rat nephron. J Am Soc Nephrol 13: 1999–2008, 2002.[Abstract/Free Full Text]
12. Endeward V, Cartron JP, Ripoche G, Gros G. Red cell membrane CO₂ permeability in normal human blood and in blood deficient in various blood groups, and effect of DIDS. Transfus Clin Biol 13: 123–127, 2006.[CrossRef][Web of Science][Medline]
13. Evans DH, Cameron JN. Gill ammonia transport. J Exp Zool 239: 17–23, 1986.[CrossRef][Web of Science]
14. Frick NT, Wright PA. Nitrogen metabolism and excretion in the mangrove killifish, Rivulus marmoratus. I. The influence of environmental salinity and external ammonia. J Exp Biol 205: 79–89, 2002.[Abstract/Free Full Text]
15. Fromm PO. Studies on renal and extra-renal excretion in a freshwater teleost, Salmo gairdneri. Comp Biochem Physiol 10: 121–128, 1963.[Medline]
16. Galvez F, Reid SD, Hawkings G, Goss GG. Isolation and characterization of mitochondria-rich cell types from the gill of freshwater rainbow trout. Am J Physiol Regul Integr Comp Physiol 282: R658–R668, 2002.[Abstract/Free Full Text]
17. Hall TA.BioEdit: a user-friendly biological sequence alignment editor and analysis program for Windows 95/98/NT. Nucleic Acids Symp Ser 41: 95–98. 1999.
18. Henry RP. Techniques for measuring carbonic anhydrase activity in vitro: the electrometric delta pH and pH stat assay. In: The Carbonic Anhydrases: Cellular Physiology and Molecular Genetics, edited by Dodgson, SJ, Tashian RE, Gros G, Carter ND. New York: Plenum, 1991, p. 119–126.
19. Huang CH, Liu PZ. New insights into the Rh superfamily of genes and proteins in erythroid cells and nonerythroid tissues. Blood Cells Mol Dis 27: 90–101, 2001.[CrossRef][Web of Science][Medline]
20. Huang CH, Peng J. Evolutionary conservation and diversification of Rh family genes and proteins. Proc Natl Acad Sci USA 102: 15512–15517, 2005.[Abstract/Free Full Text]
21. Hung CYC, Tsui KNT, Wilson JM, Nawata CM, Wood CM, Wright PA. Rhesus glycoprotein gene expression in the mangrove killifish Kryptolebias marmoratus exposed to elevated environmental ammonia levels and air. J Exp Biol 210: 2419–2429, 2007.[Abstract/Free Full Text]
22. Javelle A, Lupo D, Li XD, Merrick M, Chami M, Ripoche P, Winkler FK. Structural and mechanistic aspects of Amt/Rh proteins. J Struct Biol 158: 472–481, 2007.[CrossRef][Web of Science][Medline]
23. Juretic D, Zoranic L, Zucic D. Basic charge clusters and prediction of membrane protein topology. J Chem Inf Comput Sci 42: 620–632, 2002.[CrossRef][Web of Science][Medline]
24. Khademi S, O'Connell J III, Remis J, Robles-Colmenares Y, Mierke LJW, Stroud RM. Mechanism of ammonia transport by Amt/MEP/Rh: structure of AmtB at 1.35 . Science 305: 1587–1594, 2004.[Abstract/Free Full Text]
25. Khademi S, Stroud RM. The AmtB and the mechanism of ammonia gas conduction. Physiology 21: 419–429, 2006.[Abstract/Free Full Text]
26. Kirschner LB, Greenwald L, Kerstetter TH. Effect of amiloride on sodium transport across body surfaces of fresh water animals. Am J Physiol 224: 832–837, 1973.[Free Full Text]
27. Kumar S, Tamura K, Nei M. MEGA3: Integrated software for molecular evolutionary genetics analysis and sequence alignment. Brief Bioinform 5: 150–163, 2004.[Abstract/Free Full Text]
28. Kustu S, Inwood W. Biological gas channels for NH₃ and CO₂: evidence that Rh (Rhesus) proteins are CO₂ channels. Transfus Clin Biol 13: 103–110, 2006.[CrossRef][Web of Science][Medline]
29. Lin H, Pfeiffer DC, Wayne VA, Pan J, Randall DJ. Immunolocalization of H⁺-ATPase in the gill epithelia of rainbow trout. J Exp Biol 195: 169–183, 1994.[Abstract]
30. Lin H, Randall DJ. The effect of varying water pH on the acidification of expired water in rainbow trout. J Exp Biol 141: 14–160, 1990.
31. Lin H, Randall DJ. Evidence for the presence of an electrogenic proton pump on the trout gill epithelium. J Exp Biol 161: 119–134, 1991.[Abstract/Free Full Text]
32. Lin H, Randall DJ. H⁺-ATPase activity in crude homogenates of fish gill tissue: inhibitor sensitivity and environmental and hormonal regulation. J Exp Biol 180: 163–174, 1993.[Abstract]
33. Litwiller SL, O'Donnell MJ, Wright PA. Rapid increase in the partial pressure of NH₃ on the cutaneous surface of air-exposed mangrove killifish, Rivulus marmoratus. J Exp Biol 209: 1737–1745, 2006.[Abstract/Free Full Text]
34. Liu Z, Chen Y, Mo R, Hui C, Cheng JF, Mohandas N, Huang CH. Characterization of human RhCG and mouse Rhcg as novel nonerythroid Rh glycoprotein homologues predominantly expressed in kidney and testis. J Biol Chem 275: 25641–25651, 2000.[Abstract/Free Full Text]
35. Liu Z, Peng J, Mo R, Hui C, Huang CH. Rh type B glycoprotein is a new member of the Rh superfamily and a putative ammonia transporter in mammals. J Biol Chem 276: 1424–1438, 2001.[Abstract/Free Full Text]
36. Lumsden JS, Wright P, Derksen J, Byrne PJ, Ferguson HW. Paralysis in farmed Arctic char (Salvelinus alpinus) associated with ammonia toxicity. Vet Rec 133: 422–423, 1993.[Web of Science][Medline]
37. Mallery CH.A carrier enzyme basis for ammonium excretion in teleost gill. NH₄⁺-stimulated Na-dependent ATPase activity in Opsanus beta. Comp Biochem Physiol 74A: 889–897, 1993.
38. Marini AM, Boeckstaens M, Benjelloun F, Chérif-Zahar B, André B. Structural involvement in substrate recognition of an essential aspartate residue conserved in Mep/Amt and Rh-type ammonium transporters. Curr Genet 49: 364–374, 2006.[CrossRef][Web of Science][Medline]
39. Marini AM, Matassi G, Raynal V, André B, Cartron JP, Chérif-Zahar B. The human Rhesus-associated RhAG protein and a kidney homologue promote ammonium transport in yeast. Nat Genet 26: 341–344, 2000.[CrossRef][Web of Science][Medline]
40. Marini AM, Urrestarazu A, Beauwens R, André B. The Rh (Rhesus) blood group polypeptides are related to NH₄⁺ transporters. Trends Biochem Sci 22: 460–461, 1997.[CrossRef][Web of Science][Medline]
41. Marini AM, Vissers S, Urrestarazu A, André (1994) B. Cloning and expression of the MEP1 gene encoding an ammonium transporter of Saccharomyces cerevisiae. EMBO J 13: 3456–3463, 1994.[Web of Science][Medline]
42. Marshall WS, Bryson SE.Transport mechanisms of seawater teleost chloride cells: an inclusive model of a multifunctional cell. Comp Biochem Physiol 119A: 97–106, 1998.
43. Mazumder B, Seshadri V, Fox PL. Translational control by the 3'- UTR: the ends specify the means. Trends Biochem Sci 28: 91–98, 2003.[CrossRef][Web of Science][Medline]
44. McCormick SD. Methods for the nonlethal gill biopsy and measurements of Na⁺, K⁺-ATPase activity. Can J Fish Aquat Sci 50: 656–658, 1993.[CrossRef]
45. Mommsen TP, Walsh PJ. Biochemical and environmental perspectives on nitrogen metabolism in fishes. Experientia 48: 583–593, 1992.[CrossRef][Web of Science]
46. Murray BW, Busby ER, Mommsen TP, Wright PA. Evolution of glutamine synthetase in vertebrates: multiple glutamine synthetase genes expressed in rainbow trout (Oncorhynchus mykiss). J Exp Biol 206: 1511–1521, 2003.[Abstract/Free Full Text]
47. Nakada T, Westhoff CM, Kato A, Hirose S. Ammonia secretion from fish gill depends on a set of Rh proteins. FASEB J 21: 1–8, 2007.[Free Full Text]
48. Ninnemann O, Jauniaux JC, Frommer WB. Identification of a high affinity NH₄⁺ transporter from plants. EMBO J 13: 3464–3471, 1994.[Web of Science][Medline]
49. Playle RC, Wood CW.Water chemistry changes in the gill microenvironment of rainbow trout: experimental observations and theory. J Comp Physiol 159B: 527–537, 1989.
50. Randall DJ, Wilson JM, Peng KW, Kwok TWK, Kuah SSL, Chew SF, Lam TJ, Ip YK. The mudskipper, Periophthalmodon schlosseri, actively transports NH₄⁺ against a concentration gradient. Am J Physiol Regul Integr Comp Physiol 277: R1562–R1567, 1999.[Abstract/Free Full Text]
51. Randall DJ, Wright PA. The interaction between carbon dioxide and ammonia excretion and water pH in fish. Can J Zool 67: 2936–2942, 1987.
52. Rice P, Longden I, Bleasby A. EMBOSS: The European Molecular Biology Open Software Suite. Trends Genet 16: 276–277, 2000.[CrossRef][Web of Science][Medline]
53. Ripoche P, Bertrand O, Gane P, Birkenmeier Colin Y, Cartron JP. Human role of RhAG and AQP1 in NH₃ and CO₂ gas transport in red cell ghosts: a stopped-flow analysis. Transfus Clin Biol 13: 117–122. 2006.[CrossRef][Web of Science][Medline]
54. Salama A, Morgan IJ, Wood CM. The linkage between Na⁺ uptake and ammonia excretion in rainbow trout: kinetic analysis, the effects of (NH₄)₂SO₄ and NH₄HCO₃ infusion and the influence of gill boundary layer pH. J Exp Biol 202: 697–709, 1999.[Abstract]
55. Seshadri RM, Klein JD, Smith T, Sands JM, Handlogten ME, Verlander JW, Weiner ID. Changes in subcellular distribution of the ammonia transporter, Rhcg, in response to chronic metabolic acidosis. Am J Physiol Renal Physiol 290: F1443–F1452, 2006.[Abstract/Free Full Text]
56. Soupene E, Inwood W, Kustu S. Lack of the Rhesus protein Rh1 impairs growth of the green alga Chlamydomonas reinhardtii at high CO₂. Proc Natl Acad Sci USA 101: 7787–7792, 2004.[Abstract/Free Full Text]
57. Thompson JD, Higgins DG, Gibson TJ. CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice. Nucleic Acids Res 22: 4673–4680, 1994.[Abstract/Free Full Text]
58. Verdouw H, van Echteld CJA, Dekkers EMJ. Ammonia determinations based on indophenol formation with sodium salicylate. Water Res 12: 399–402, 1978.
59. Weiner ID, Hamm LL.Molecular mechanisms of renal ammonia transport. Annu Rev Physiol 69: 3.1–3.24, 2006.
60. Westhoff CM. The structure and function of the Rh antigen complex. Semin Hematol 44: 42–50, 2007.[CrossRef][Web of Science][Medline]
61. Westhoff CM, Wylie DE. Transport characteristics of mammalian Rh and Rh glycoproteins expressed in heterologous systems. Transfus Clin Biol 13: 132–138, 2006.[CrossRef][Web of Science][Medline]
62. Wilkie MP. Ammonia excretion and urea handling by fish gills: present understanding and future research challenges. J Exp Zool 293: 284–301, 2002.[CrossRef][Web of Science][Medline]
63. Wilson RW, Taylor EW. Transbranchial ammonia gradients and acid-base responses to high external ammonia concentration in rainbow trout (Oncorhynchus mykiss) acclimated to different salinities. J Exp Biol 166: 95–112, 1992.[Abstract/Free Full Text]
64. Wilson RW, Wright PM, Munger S, Wood CM. Ammonia excretion in fresh water rainbow trout (Oncorhynchus mykiss) and the importance of gill boundary layer acidification: lack of evidence for Na⁺/NH₄⁺ exchange. J Exp Biol 191: 37–58, 1994.[Abstract]
65. Wittbrodt J, Meyer A, Schartl M. More genes in fish? Bioessays 20: 511–515, 1998.[CrossRef][Web of Science]
66. Wolf K. Physiological salines for fresh water teleosts. Progve Fish Cult 25: 135–140, 1963.
67. Wood CM. Ammonia and urea metabolism and excretion. In: The Physiology of Fishes, edited by Evans D. Boca Raton, FL: CRC, 1993, p. 379–425.
68. Wright PA, Heming T, Randall DJ. Downstream pH changes in water flowing over the gills of rainbow trout. J Exp Biol 126: 499–512, 1986.[Abstract/Free Full Text]
69. Wright PA, Randall DJ, Perry SF. Fish gill boundary layer: a site of linkage between carbon dioxide and ammonia excretion. J Comp Physiol 158: 627–635, 1989.[CrossRef]
70. Wright PA, Wood CM. An analysis of branchial ammonia excretion in the freshwater rainbow trout: effects of environmental pH change and sodium uptake blockage. J Exp Biol 114: 329–353, 1985.[Abstract/Free Full Text]
71. Zheng L, Kostrewa D, Berneche S, Winkler FK, Li XD. The mechanism of ammonia transport based on the crystal structure of AmtB of Escherichia coli. Proc Natl Acad Sci USA 101: 17090–17095, 2004.[Abstract/Free Full Text]
72. Zidi-Yahiaoui N, Ripoche P, Van Kim CL, Gane P, D'Ambrosio AM, Cartron JP, Colin Y, Mouro-Chanteloup I. Ammonium transport properties of HEK293 cells expressing RhCG mutants: preliminary analysis of structure/function by site-directed mutagenensis. Transfus Clin Biol 13: 128–131, 2006.[CrossRef][Web of Science][Medline]

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